CD8+/perforin+/WC1- γδ T cells, not CD8+ αβ T cells, infiltrate vasculitis lesions of American bison (Bison bison) with experimental sheep-associated malignant catarrhal fever

Veterinary Immunology and Immunopathology

Volumn 136, Issue 3-4, 2010, Pages 284-291

  Nelson, Danielle D ^a   Davis, William C ^a   Brown, Wendy C ^a   Li, Hong ^a,b   O'Toole, Donal ^c   Oaks, J Lindsay ^a  

^a WASHINGTON STATE UNIVERSITY   (United States)

^b AGRICULTURAL RESEARCH SERVICE   (United States)

^c UNIVERSITY OF WYOMING   (United States)

Author keywords

Herpesvirus; d T cells; Bison; Malignant catarrhal fever; Vasculitis

Indexed keywords

CD8 ANTIGEN; PERFORIN; PROTEIN; UNCLASSIFIED DRUG; WC1 PROTEIN; LYMPHOCYTE ANTIGEN RECEPTOR;

ALPHA BETA T LYMPHOCYTE; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; B LYMPHOCYTE; BLADDER; BUFFALO; CD8+ T LYMPHOCYTE; CONTROLLED STUDY; CYTOTOXIC T LYMPHOCYTE; GAMMA DELTA T LYMPHOCYTE; IMMUNOPHENOTYPING; INNATE IMMUNITY; KIDNEY; LIVER; MALE; MALIGNANT CATARRHAL FEVER; NONHUMAN; PATHOGENESIS; SHEEP ASSOCIATED MALIGNANT CATARRHAL FEVER; T LYMPHOCYTE; VASCULITIS; ANIMAL; ANIMAL DISEASE; FLUORESCENCE MICROSCOPY; GAMMAHERPESVIRINAE; HERPES VIRUS INFECTION; IMMUNOLOGY; METHODOLOGY; VIROLOGY;

BISON; BISON BISON; BOS; HERPESVIRIDAE; OVINE HERPESVIRUS 2; OVIS ARIES;

ANIMALS; BISON; CD8-POSITIVE T-LYMPHOCYTES; GAMMAHERPESVIRINAE; HERPESVIRIDAE INFECTIONS; IMMUNOPHENOTYPING; MALE; MALIGNANT CATARRH; MICROSCOPY, FLUORESCENCE; PERFORIN; RECEPTORS, ANTIGEN, T-CELL, GAMMA-DELTA; T-LYMPHOCYTES, CYTOTOXIC; VASCULITIS;

EID: 77958159809     PISSN: 01652427     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.vetimm.2010.03.023     Document Type: Article

References (55)

1. Anderson I.E., Buxton D., Campbell I., Russell G., Davis W.C., Hamilton M.J., Haig D.M. Immunohistochemical study of experimental malignant catarrhal fever in rabbits. J. Comp. Pathol. 2007, 136:156-166.
2. Anderson I.E., Deane D., Swa S., Thomson J., Campbell I., Buxton D., Wei X.Q., Stewart J., Russell G., Haig D.M. Production and utilization of IL-15 in malignant catarrhal fever. J. Comp. Pathol. 2008, 138:131-144.
3. Baldwin C.L., Teale A.J., Naessens J.G., Goddeeris B.M., MacHugh N.D., Morrison W.I. Characterization of a subset of bovine T lymphocytes that express BoT4 by monoclonal antibodies and function: similarity to lymphocytes defined by human T4 and murine L3T4. J. Immunol. 1986, 136:4385-4391.
4. Berezowski J.A., Appleyard G.D., Crawford T.B., Haigh J., Li H., Middleton D.M., O'Connor B.P., West K., Woodbury M. An outbreak of sheep-associated malignant catarrhal fever in bison (Bison bison) after exposure to sheep at a public auction sale. J. Vet. Diagn. Invest. 2005, 17:55-58.
5. Burrells C., Reid H.W. Phenotypic analysis of lymphoblastoid cell lines derived from cattle and deer affected with " sheep-associated" malignant catarrhal fever. Vet. Immunol. Immunopathol. 1991, 29:151-161.
6. Buser R., Montesano R., Garcia I., Dupraz P., Pepper M.S. Bovine microvascular endothelial cells immortalized with human telomerase. J. Cell. Biochem. 2006, 98:267-286.
7. Chen Z., Freedman M. CD16+ gammadelta T cells mediate antibody dependent cellular cytotoxicity: potential mechanism in the pathogenesis of multiple sclerosis. Clin. Immunol. 2008, 128:219-227.
8. Clevers H. Identification of a bovine surface antigen uniquely expressed on CD4-CD8- T cell receptor gamma/delta+ T lymphocytes. Eur. J. Immunol. 1990, 20:809-817.
9. Cook C.G., Splitter G.A. Lytic function of bovine lymphokine-activated killer cells from a normal and a malignant catarrhal fever virus-infected animal. Vet. Immunol. Immunopathol. 1988, 19:105-118.
10. Crawford T.B., O'Toole D., Li H. Malignant catarrhal fever. Current Veterinary Therapy. IV: Food Animal Practice 1998, 306-309. W.B. Saunders Company, Philadelphia, PA. R.A. Smith, J.L. Howard (Eds.).
11. Crocker P.J., Jefferies W.A., Clark S.J., Chung L.P., Gordon S. Species heterogeneity in macrophage expression of the CD4 antigen. J. Exp. Med. 1987, 166:613-618.
12. Davis W.C. The use of crossreactive monoclonal antibodies to characterize the immune system of the water buffalo (Bubalus bubalis). J. Vet. Sci. 2001, 2:103-109.
13. Davis W.C., Brown W.C., Hamilton M.J., Wyatt C.R., Orden J.A., Khalid A.M., Naessens J. Analysis of monoclonal antibodies specific for the gammadelta TcR. Vet. Immunol. Immunopathol. 1996, 52:275-283.
14. Ellis J.A., O'Toole D.T., Haven T.R., Davis W.C. Predominance of BoCD8-positive T lymphocytes in vascular lesions in a 1-year-old cow with concurrent malignant catarrhal fever and bovine viral diarrhea virus infection. Vet. Pathol. 1992, 29:545-547.
15. Endsley J.J. Bovine natural killer cells acquire cytotoxic/effector activity following activation with IL-12/15 and reduce Mycobacterium bovis BCG in infected macrophages. J. Leukoc. Biol. 2006, 79:71-79.
16. Endsley J.J., Furrer J.L., Endsley M.A., McIntosh M.A., Maue A.C., Waters W.R., Lee D.R., Estes D.M. Characterization of bovine homologues of granulysin and NK-lysin. J. Immunol. 2004, 173:2607-2614.
17. Endsley J.J., Hogg A., Shell L.J., McAulay M., Coffey T., Howard C., Capinos Scherer C.F., Waters W.R., Nonnecke B., Estes D.M., Villarreal-Ramos B. Mycobacterium bovis BCG vaccination induces memory CD4+ T cells characterized by effector biomarker expression and anti-mycobacterial activity. Vaccine 2007, 25:8384-8394.
18. Galeotti M., Sarli G., Eleni C., Marcato P.S. Identification of cell types present in bovine haemolymph nodes and lymph nodes by immunostaining. Vet. Immunol. Immunopathol. 1993, 36:319-331.
19. Gunnes G., Jorundsson E., Tverdal A., Landsverk T., Press C.M. Accumulation of CD25+ CD4+ T-cells in the draining lymph node during the elicitation phase of DNCB-induced contact hypersensitivity in lambs. Res. Vet. Sci. 2004, 77:115-122.
20. Gutierrez M., Forster F.I., McConnell S.A., Cassidy J.P., Pollock J.M., Bryson D.G. The detection of CD2+, CD4+, CD8+, and WC1+ T lymphocytes, B cells and macrophages in fixed and paraffin embedded bovine tissue using a range of antigen recovery and signal amplification techniques. Vet. Immunol. Immunopathol. 1999, 71:321-334.
21. Halary F., Pitard V., Dlubek D., Kryzsiek R., de la Salle H., Merville P., Dromer C., Emilie D., Moreau J.-F., Dechanet-Merville J. Shared reactivity of Vdelta2 negative gammadelta T cells against cytomegalovirus-infected cells and tumor intestinal epithelial cells. J. Exp. Med. 2005, 201:1567-1578.
22. Hedges J.F., Lubick K.J., Jutila M.A. Gamma delta T cells respond directly to pathogen-associated molecular patterns. J. Immunol. 2005, 174:6045-6053.
23. Horner G.W., Tham K.M., Orr D., Ralston J., Rowe S., Houghton T. Comparison of an antigen capture enzyme-linked assay with reverse transcription-polymerase chain reaction and cell culture immunoperoxidase tests for the diagnosis of ruminant pestivirus infections. Vet. Microbiol. 1995, 43:75-84.
24. Hussy D., Stauber N., Leutenegger C.M., Rieder S., Ackermann M. Quantitative fluorogenic PCR assay for measuring ovine herpesvirus 2 replication in sheep. Clin. Diagn. Lab. Immunol. 2001, 8:123-128.
25. Jeklova E., Leva L., Faldyna M. Lymphoid organ development in rabbits: major lymphocyte subsets. Dev. Comp. Immunol. 2007, 31:632-644.
26. Jutila M.A., Holderness J., Graff J.C., Hedges J.F. Antigen-independent priming: a transitional response of bovine gamma delta T cells to infection. Anim. Health Res. Rev. 2008, 9:47-57.
27. Kramps J.A., van Maanen C., van de Wetering G., Stienstra G., Quak S., Brinkhof J., Ronsholt L., Nylin B. A simple, rapid and reliable enzyme-linked immunosorbent assay for the detection of bovine virus diarrhoea virus (BVDV) specific antibodies in cattle serum, plasma and bulk milk. Vet. Microbiol. 1999, 64:135-144.
28. Lagourette P., Delverdier M., Bourges-Abella N., Amardeilh M.F., Schelcher F., Cabanie P., Espinasse J. Immunohistochemical study of lymphoid cell reactions in four cattle affected with malignant catarrhal fever. Eur. J. Vet. Pathol. 1997, 3:73-78.
29. Li H. A devastating outbreak of malignant catarrhal fever in a bison feedlot. J. Vet. Diagn. Invest. 2006, 18:119-123.
30. Li H., McGuire T.C., Muller-Doblies U.U., Crawford T.B. A simpler, more sensitive competitive inhibition enzyme-linked immunosorbent assay for detection of antibody to malignant catarrhal fever viruses. J. Vet. Diagn. Invest. 2001, 13:361-364.
31. Li H., Shen D.T., O'Toole D., Knowles D.P., Gorham J.R., Crawford T.B. Investigation of sheep-associated malignant catarrhal fever virus infection in ruminants by PCR and competitive inhibition enzyme-linked immunosorbent assay. J. Clin. Microbiol. 1995, 33:2048-2053.
32. Li H., Karney G., O'Toole D., Crawford T.B. Long distance spread of malignant catarrhal fever virus from feedlot lambs to ranch bison. Can. Vet. J. 2008, 49:183-185.
33. Liggitt H.D. The pathomorphology of malignant catarrhal fever. I. Generalized lymphoid vasculitis. Vet. Pathol. 1980, 17:58-72.
34. MacHugh N.D. Analysis of the reactivity of anti-bovine CD8 monoclonal antibodies with cloned T cell lines and mouse L-cells transfected with bovine CD8. Vet. Immunol. Immunopathol. 1991, 27:169-172.
35. MacHugh N.D., Mburu J.K., Carol M.J., Wyatt C.R., Orden J.A., Davis W.C. Identification of two distinct subsets of bovine gammadelta T cells with unique cell surface phenotype and tissue distribution. Immunology 1997, 92:340-345.
36. MacHugh N.D., Mburu J.K., Hamilton M.J., Davis W.C. Characterisation of a monoclonal antibody recognising the CD3[var epsilon] chain of the bovine T cell receptor complex. Vet. Immunol. Immunopathol. 1998, 61:25-35.
37. Marks L. The cytotoxic potential of regulatory T cells: what has been learned from gene knockout model systems?. Transplantation 2004, 77:S19-S22.
38. Meissner N., Radke J., Hedges J.F., White M., Behnke M., Bertolino S., Abrahamsen M., Jutila M.A. Serial analysis of gene expression in circulating gammadelta T cell subsets defines distinct immunoregulatory phenotypes and unexpected gene expression profiles. J. Immunol. 2003, 170:356-364.
39. Nakajima Y., Ishikawa Y., Kadota K., Kodama M., Honma Y. Surface marker analysis of the vascular and epithelia lesions in cattle with sheep-associated malignant catarrhal fever. J. Vet. Med. Sci. 1994, 56:1065-1068.
40. O'Toole D., Taus N.S., Montgomery D.L., Oaks J.L., Crawford T.B., Li H. Intra-nasal inoculation of American Bison (Bison bison) with ovine herpesvirus-2 (OvHV-2) reliably reproduces malignant catarrhal fever. Vet. Pathol. 2007, 44:655-662.
41. Parsons K.R. Identification of a molecule uniquely expressed on a gamma/delta TCR+ subset within bovine intestinal intraepithelial lymphocytes. Immunology 1996, 87:64-70.
42. Plowright W. Malignant catarrhal fever virus. Virus Infections of Ruminants 1990, 123-150. Elsevier Science Publishers, BV, New York, NY. Z. Dinter, B. Morein (Eds.).
43. Reid H.W., Buxton D., Pow I., Finlayson J. Isolation and characterisation of lymphoblastoid cells from cattle and deer affected with 'sheep-associated' malignant catarrhal fever. Res. Vet. Sci. 1989, 47:90-96.
44. Schock A., Collins R.A., Reid H.W. Phenotype, growth regulation and cytokine transcription in ovine herpesvirus-2 (OHV-2)-infected bovine T-cell lines. Vet. Immunol. Immunopathol. 1998, 66:67-81.
45. Schultheiss P.C., Collins J.K., Austgen L.E., DeMartini J.C. Malignant catarrhal fever in bison, acute and chronic cases. J. Vet. Diagn. Invest. 1998, 10:255-262.
46. Schultheiss P.C., Collins J.K., Spraker T.R., DeMartini J.C. Epizootic malignant catarrhal fever in three bison herds: differences from cattle and association with ovine herpesvirus-2. J. Vet. Diagn. Invest. 2000, 12:497-502.
47. Simon S., Li H., O'Toole D., Crawford T.B., Oaks J.L. The vascular lesions of a cow and bison with sheep-associated malignant catarrhal fever contain ovine herpesvirus 2-infected CD8(+) T lymphocytes. J. Gen. Virol. 2003, 84:2009-2013.
48. Sopp P., Kwong L.S., Howard C.J. Identification of bovine CD14. Vet. Immunol. Immunopathol. 1996, 52:323-328.
49. Storset A.K. NKp46 defines a subset of bovine leukocytes with natural killer cell characteristics. Eur. J. Immunol. 2004, 34:669-676.
50. Taus N.S., Traul D.L., Oaks J.L., Crawford T.B., Lewis G.S., Li H. Experimental infection of sheep with ovine herpesvirus 2 via aerosolization of nasal secretions. J. Gen. Virol. 2005, 86:575-579.
51. Trueblood E.S., Brown W.C., Palmer G.H., Davis W.C., Stone D.M., McElwain T.F. B-lymphocyte proliferation during bovine leukemia virus induced persistent lymphocytosis is enhanced by T-lymphocyte-derived interleukin-2. J. Virol. 1998, 72:3169-3177.
52. Wangoo A., Johnson L., Gough J., Ackbar R., Inglut S., Hicks D., Spencer Y., Hewinson G., Vordermeier M. Advanced granulomatous lesions in Mycobacterium bovis-infected cattle are associated with increased expression of type I procollagen, gammadelta (WC1+) T cells and CD 68+ cells. J. Comp. Pathol. 2005, 133:223-234.
53. Warren A.L., Summers B.A. Epithelioid variant of hemangioma and hemangiosarcoma in the dog, horse, and cow. Vet. Pathol. 2007, 44:15-24.
54. Weiss D.J. Mucosal immune response in cattle with subclinical Johne's disease. Vet. Pathol. 2006, 43:127-135.
55. Wilson E., Hedges J.F., Butcher E., Briskin M., Jutila M.A. Bovine gammadelta T cell subsets express distinct patterns of chemokine responsiveness and adhesion molecules: a mechanism for tissue-specific gammadelta T cell subset accumulation. J. Immunol. 2002, 169:4970-4975.